Variant #0000547300 (NC_000012.11:g.15702179_15702180insAAA, NC_000012.11(NM_002848.3):c.2437+19_2437+20insAAA (PTPRO))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.15702179_15702180insAAA
DNA change (hg38) g.15549245_15549246insAAA
Published as PTPRO(NM_030667.3):c.2437+19_2437+20insAAA
ISCN -
DB-ID PTPRO_000020
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00301 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTPRO NM_002848.3 -?/. - c.2437+19_2437+20insAAA r.(=) p.(=)


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